新产品编号:2326049
Chemical Name: (6aR,7S,9aS,11S,13aS)-3-Imino-6a,7,10,10-tetramethyl-2,3,6,6a,7,8,9,9a,10,11,12,13-dodecahydro-1H-naphtho[1',8a':5,6]pyran[2,3-e]isoindole-5,11-diol hydrochloride
项目整合开发状态: Biological Testing
项目研究机构: Shionogi (Originator)
合成路线:The title compound was prepared using acetylstachyflin (I),a fermentation product from Stachybotrys sp.RF-7260,as the starting material.After protection of the phenolic hydroxyl group of (I) as the benzyl ether (II),alcoholysis of its acetate ester with methanolic NaOMe yielded alcohol (III).Oxidation of the secondary alcohol (III) by means of Jones reagent gave rise to ketone (IV).The O-benzyl group of (IV) was finally removed by hydrogenolysis over Pd/C to produce the desired phenol.
合成路线:Compound SQ-02-S-V2 (I) is isolated from the fermentation broths of Stachybotrys sp.RF-7260 under modified conditions in the presence of DL-valine.Subsequent,methanolysis of the acetate ester group of (I) in the presence of NaOMe gives rise to the title compound.
📌 参考资料/链接:
参考文献标题:Sesquiterpene derivs.having antiviral activity
文献作者:Kamigauchi,T.; Fujiwara,T.; Tani,H.; Kawamura,Y.; Horibe,I.(Shionogi & Co.Ltd.)
参考来源:EP 0855398; WO 9711947
📄 详细内容
合成路线:Compound SQ-02-S-V2 (I) is isolated from the fermentation broths of Stachybotrys sp.RF-7260 under modified conditions in the presence of DL-valine.Subsequent,methanolysis of the acetate ester group of (I) in the presence of NaOMe gives rise to the title compound.
参考文献标题:Novel stachyflin derivatives from Stachybotrys sp.RF-7260.Fermentation,isolation,structure elucidation and biological activities
文献作者:Minagawa,K.; Kouzuki,S.; Tani,H.; Ishii,K.; Tanimoto,T.; Terui,Y.; Kamigauchi,T.
参考来源:J Antibiot 2002,55(3),239